"69336-112-30" National Drug Code (NDC)

NDC Code	69336-112-30
Package Description	30 CAPSULE in 1 PACKAGE (69336-112-30)
Product NDC	69336-112
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Not Applicable
Non-Proprietary Name	Omeprazole Sodium Bicarbonate
Dosage Form	CAPSULE
Usage	ORAL
Start Marketing Date	20170713
Marketing Category Name	ANDA
Application Number	ANDA207476
Manufacturer	Sterling Knight Pharmaceuticals LLC
Substance Name	OMEPRAZOLE; SODIUM BICARBONATE
Strength	40; 1100
Strength Unit	mg/1; mg/1
Pharmacy Classes	Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA],Cytochrome P450 2C19 Inhibitors [MoA],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA]